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Abstract

Contamination of drinking groundwater with arsenic is a looming problem in several countries and has affected millions of people, distributed over some 20 countries, globally including people in West Bengal (India) and Bangladesh. Continued exposure to Arsenic (‘As’) leads to various disorders and malfunctioning of renal, reproductive, cardiovascular and respiratory system along with the lethal effects manifested on skin and epidermal cells. In the review, an effort was made to incorporate the findings of other investigators and to evaluate the relation among arsenic metabolism and the consequences of numerous chronic disease. Early indications/manifestations of arsenicosis is difficult because of the occurrence of non-specific symptoms in various water-borne ailments. It has emerged that orthodox drugs used for treating arsenicosis was highly unsatisfactory as they have their own toxic side effects. In such a scenario, insights to the biological and epidemiological meanings of arsenic metabolism can help in mitigating the risk of arsenic toxicity and provide a prospective means for disease prophecy, prevention and control.

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Abbreviations

As:

Arsenic

AsIII:

Arsenite

AsV:

Arsenate

DMAV:

Dimethylarsinic

DMAIII:

Dimethyl arsinous

MMAV:

Monomethyl arsonic

MMAIII:

Monomethyl arsonous

ROS:

Reactive oxygen species

References

  • Abbott, N., Rönnbäck, L., & Hansson, E. (2006). Astrocyte–endothelial interactions at the blood–brain barrier. Nature Reviews Neuroscience, 7, 41–53.

    Article  Google Scholar 

  • Aggarwal, M., Naraharisetti, S. B., Dandapat, S., Degen, G. H., & Malik, J. K. (2008). Perturbations in immune responses induced by concurrent sub-chronic exposure to arsenic and endosulfan. Toxicology, 251(1–3), 51–60.

    Article  Google Scholar 

  • Ahmed, F., & Rahman, M. (2003). Low-cost water supply technologies. In: F. Ahmed & M. Rahman (Eds.), Water supply and sanitation. Rural and low-income urban Communities. ITN-Bangladesh, Dhaka, pp. 407–441.

    Google Scholar 

  • Akram, Z., Jalali, S., Shami, S. A., Ahmad, L., Batool, S., & Kalsoom, O. (2009). Genotoxicity of sodium arsenite and DNA fragmentation in ovarian cells of rat. Toxicology Letters, 190(1), 81–85.

    Article  Google Scholar 

  • Aksakal, O., & Esim, N. (2015). Evaluation of arsenic trioxide genotoxicity in wheat seedlings using oxidative system and RAPD assays. Environmental Science Pollution Research International, 22(9), 7120–7128.

    Article  Google Scholar 

  • Allen, T., & Rana, S. V. (2007). Effect of n-propylthiouracil or thyroxine on arsenic trioxide toxicity in the liver of rat. Journal of Trace Elements in Medicine and Biology, 21(3), 194–203.

    Article  Google Scholar 

  • Ambrosio, F., Brown, E., Stolz, D., Ferrari, R., Goodpaster, B., Deasy, B., et al. (2014). Arsenic induces sustained impairment of skeletal muscle and muscle progenitor cell ultrastructure and bioenergetics. Free Radical Biology and Medicine, 74, 64–73.

    Article  Google Scholar 

  • Arnold, L. L., Eldan, M., van Gemert, M., Capen, C. C., & Cohen, S. M. (2003). Chronic studies evaluating the carcinogenicity of monomethylarsonic acid in rats and mice. Toxicology, 190(3),197–219.

    Google Scholar 

  • ATSDR. (2007). Agency for toxic substances and disease registry. Toxicological profile for arsenic. Draft for Public Comment. Atlanta GA. www.atsdr.cdc.gov/toxprofiles.

  • Baastrup, R., Sørensen, M., Balstrøm, T., Frederiksen, K., Larsen, C. L., Tjønneland, A., et al. (2008). Arsenic in drinking-water and risk for cancer in Denmark. Environmental Health Perspectives, 116(2), 231–237.

    Article  Google Scholar 

  • Bailey, K. A., Wu, M. C., Ward, W. O., Smeester, L., Rager, J. E., García-Vargas, G., et al. (2013). Arsenic and the epigenome: Interindividual differences in arsenic metabolism related to distinct patterns of DNA methylation. Journal of Biochemical and Molecular Toxicology, 27(2), 106–115.

    Article  Google Scholar 

  • Banerjee, M., Banerjee, N., Ghosh, P., Das, J. K., Basu, S., Sarkar, A. K., et al. (2010). Evaluation of the serum catalase and myeloperoxidase activities in chronic arsenic-exposed individuals and concomitant cytogenetic damage. Toxicology Applied Pharmacology, 249(1), 47–54.

    Article  Google Scholar 

  • Banerjee, N., Banerjee, S., Sen, R., Bandyopadhyay, A., Sarma, N., Majumder, P., et al. (2009). Chronic arsenic exposure impairs macrophage functions in the exposed individuals. Journal of Clinical Immunology, 29(5), 582–594.

    Article  Google Scholar 

  • Belon, P., Banerjee, A., Karmakar, S. R., Biswas, S. J., Choudhury, S. C., Banerjee, P., et al. (2007). Homeopathic remedy for arsenic toxicity? Evidence-based findings from a randomized placebo-controlled double blind human trial. Science of Total Environment, 384(1–3), 141–150.

    Article  Google Scholar 

  • Belon, P., Banerjee, P., Choudhury, S. C., Banerjee, A., Biswas, S. J., Karmakar, S. R., et al. (2006). Can administration of potentized homeopathic remedy, Arsenicum album, alter antinuclear antibody (ANA) titer in people living in high-risk arseniccontaminated areas? I. A correlation with certain hematological parameters. Evidence-Based Complementary and Alternative Medicine, 3(1), 99–107.

    Google Scholar 

  • Bishayi, B., & Sengupta, M. (2003). Intracellular survival of Staphylococcus aureus due to alteration of cellular activity in arsenic and lead intoxicated mature Swiss albino mice. Toxicology, 184(1), 31–39.

    Article  Google Scholar 

  • Bishayi, B., & Sengupta, M. (2006). Synergism in immunotoxicological effects due to repeated combined administration of arsenic and lead in mice. International Immunopharmacology., 3, 454–464.

    Article  Google Scholar 

  • Biswas, S. J., Ghosh, G., & Dubey, V. P. (2019). Modulation of sodium arsenite-induced toxicity in mice by ethanolic seed extract of Trigonella foenum graecum. Pharmacognosy Magazine, 15, S386-395.

    Article  Google Scholar 

  • Bjørklund, G., Tippairote, T., Rahaman, M. S., & Aaseth, J. (2020). Developmental toxicity of arsenic: A drift from the classical dose–response relationship. Archives of Toxicology, 94, 67–75.

    Article  Google Scholar 

  • Chatterjee, D., Adak, S., Banerjee, N., Bhattacharjee, P., Bandyopadhyay, A. K., & Giri, A. K. (2018). Evaluatıon of health effects, genetıc damage and telomere length ın children exposed to arsenic in West Bengal, İndia. Mutation Research Genetic Toxicology Environmental Mutagenesis, 836(Pt A), 82–88.

    Article  Google Scholar 

  • Chattopadhyay, S., Ghosh, S., Chaki, S., Debnath, J., & Ghosh, D. (1999). Effect of sodium arsenite on plasma levels of gonadotrophins and ovarian steroidogenesis in mature albino rats: Duration-dependent response. The Journal of Toxicological Sciences, 24(5), 425–431.

    Article  Google Scholar 

  • Chattopadhyay, S., Pal (Ghosh), S., Ghosh, D., & Debnath, J. (2003). Effect of dietary co-administration of sodium selenite on sodium arsenite-induced ovarian and uterine disorders in mature albino rats. Toxicological Sciences, 75(2), 412–422.

    Google Scholar 

  • Chiocchetti, G. M., Vélez, D., & Devesa, V. (2019). Effect of chronic exposure to inorganic arsenic on intestinal cells. Journal of Applied Toxicology, 39(6), 899–907.

    Article  Google Scholar 

  • Chiocchetti, G. M., Vélez, D., & Devesa V. (2019b). Inorganic arsenic causes intestinal barrier disruption. Metallomics, 11(8), 1411–1418.

    Google Scholar 

  • Chou, C. J., Tsai, M. S., Tsai, J. L., Lee, H. H., & Lin, T. J. (2002). The chelating treatment is notuseful in human’s intoxication with acute herbicidal organic arsenic. Human and Experimental Toxicology, 21(12), 631–634.

    Article  Google Scholar 

  • Chow, S. K., Chan, J. Y., & Fung, K. P. (2004). Suppression of cell proliferation and regulation of estrogen receptor alpha signaling pathway by arsenic trioxide on human breast cancer MCF-7 cells. Journal of Endocrinology, 182(2), 325–337.

    Article  Google Scholar 

  • Concha, G., Nermell, B., & Vahter, M. V. (1998). Metabolism of inorganic arsenic in children with chronic high arsenic exposure in northern Argentina. Environmental Health Perspective, 106(6), 355–359.

    Article  Google Scholar 

  • da Silva, R. F., Borges, C. D. S., de Almeida Lamas, C., Cagnon, V. H. A., & de Grava Kempinas, W. (2017). Arsenic trioxide exposure impairs testicular morphology in adult male mice and consequent fetus viability. Journal of Toxicology and Environment Health A, 80(19–21), 1166–1179.

    Article  Google Scholar 

  • Dastgiri, S., Mosaferi, M., Fizi, M. A., Olfati, N., Zolali, S., Pouladi, N., & Azarfam, P. (2010). Arsenic exposure, dermatological lesions, hypertension, and chromosomal abnormalities among people in a rural community of northwest Iran. Journal of Health Population and Nutrition, 28(1), 14–22.

    Google Scholar 

  • De Loma, J., Skröder, H., Raqib, R., Vahter, M., & Broberg, K. (2018). Arsenite methyltransferase(AS3MT) polymorphisms and arsenic methylation in children in rural Bangladesh. Toxicology and Applied Pharmacology, 357, 80–87.

    Article  Google Scholar 

  • Dringen, R., Spiller, S., Neumann, S., & Koehler, Y. (2016). Uptake, metabolic effects and toxicity of arsenate and arsenite in astrocytes. Neurochemistry Research, 41(3), 465–475.

    Article  Google Scholar 

  • Dulout, F. N., Grillo, C. A., Seoane, A. I., Maderna, C. R., Nilsson, R., Vahter, M., et al. (1996). Chromosomal aberrations in peripheral blood lymphocytes from native Andean women and children from northwestern Argentina exposed to arsenic indrinking water. Mutation Research, 370(3–4), 151–158.

    Article  Google Scholar 

  • Duquesnoy, I., Champeau, G. M., Evray, G., Ledoigt, G., & Piquet-Pissaloux, A. (2010). Enzymatic adaptations to arsenic-induced oxidative stress in Zea mays and genotoxic effect of arsenic in root tips of Vicia faba and Zea mays. Comptes Rendus Biologies, 333, 814–824.

    Article  Google Scholar 

  • Ersbøll, A. K., Monrad, M., Sørensen, M., Baastrup, R., Hansen, B., Bach, F. W., et al. (2018). Low-level exposure to arsenic in drinking water and incidence rate of stroke: A cohort study in Denmark. Environment International, 120, 72–80.

    Article  Google Scholar 

  • Ferrario, D., Collotta, A., Carfi, M., Bowe, G., Vahter, M., Hartung, T., & Gribaldo, L. (2009). Arsenic induces telomerase expression and maintains telomere length in human cordblood cells. Toxicology, 260(1–3), 132–141.

    Article  Google Scholar 

  • Flanagan, S. V., Johnston, R. B., & Zheng, Y. (2012). Arsenic in tube well water in Bangladesh: Health and economic impacts and implications for arsenic mitigation. Bulletin of World Health Organization, 90(11), 839–846.

    Article  Google Scholar 

  • Francesconi, K. A., & Edmonds, J. S. (1987). The identification of arsenobetaine as the sole water-soluble arsenic constituent of the tail muscle of the western king prawn Penaeus latisulcatus. Comparative Biochemistry and Physiology C, 87(2), 345–347.

    Article  Google Scholar 

  • Ghiani, A., Fumagalli, P., Nguyen Van, T., Gentili, R., & Citterio, S. (2014). The combined toxic and genotoxic effects of Cd and As to plant bioindicator Trifolium repens L. PLoS One, 109(6), e99239. https://doi.org/10.1371/journal.pone.0099239.

  • Ghosh, D., Datta, S., Bhattacharya, S., & Mazumder, S. (2007). Long-term exposure to arsenic affects head kidney and impairs humoral immune responses of Clarias batrachus. Aquatic Toxicology, 81 (1), 79–89.

    Google Scholar 

  • Ghosh, P., Banerjee, M., De Chaudhuri, S., Chowdhury, R., Das, J. K., Mukherjee, A., et al. (2007). Comparison of health effects between individuals with and without skin lesions in the population exposed to arsenic through drinking water in West Bengal, India. Journal of Exposure Science and Environmental Epidemiology, 17(3), 215–223.

    Google Scholar 

  • Ghosh, P., Basu, A., Mahata, J., Basu, S., Sengupta, M., Das, J. K., et al. (2006). Cytogenetic damage and genetic variants in the individuals susceptible to arsenic-induced cancer through drinking water. International Journal of Cancer, 118(10), 2470–2478.

    Article  Google Scholar 

  • González-Martínez, F., Sánchez-Rodas, D., Cáceres, D. D., Martínez, M. F., Quiñones, L. A., Johnson-Restrepo, B. (2018). Arsenic exposure, profiles of urinary arsenic species, and polymorphism effects of glutathione-s-transferase and metallothioneins.Chemosphere, 212, 927–936.

    Google Scholar 

  • Greani, S., Lourkisti, R., Berti, L., Marchand, B., Giannettini, J., Santini, J., & Quilichini, Y. (2017). Effect of chronic arsenic exposure under environmental conditionson bioaccumulation, oxidative stress, and antioxidant enzymatic defenses in wild trout Salmo trutta (Pisces, Teleostei). Ecotoxicology, 26(7), 930–941.

    Article  Google Scholar 

  • Gur, E., Pirak, M., & Waner, T. (1991). Methane arsonic acid oncogenicity study in the mouse. Luxembourg Industries (Pamol) Ltd. Submitted to the U.S. Environmental Protection Agency. MRID42173201.

    Google Scholar 

  • Haque, R., Mazumder, D. N., Samanta, S., Ghosh, N., Kalman, D., Smith, M. M., et al. (2003). Arsenic in drinking water and skin lesions: Dose-response data from West Bengal, India. Epidemiology, 14(2), 174–182.

    Article  Google Scholar 

  • Hartmann, A., & Speit, G. (1996). Effect of arsenic and cadmium on the persistence of mutagen-induced DNA lesions in human cells. Environment and Molecular Mutagenesis, 27(2), 98–104.

    Article  Google Scholar 

  • Heck, J. E., Chen, Y., Grann, V. R., Slavkovich, V., Parvez, F., & Ahsan, H. (2008). Arsenic exposure and anemia in Bangladesh: A population-based study. Journal of Occupational Environmental Medicine, 50(1), 80–87.

    Article  Google Scholar 

  • Heck, J. E., Park, A. S., Qiu, J., Cockburn, M., & Ritz, B. (2014). Risk of leukemia in relation to exposure to ambient air toxics in pregnancy and early childhood. International Journal of Hygiene and Environ Health, 217(6), 662–668.

    Article  Google Scholar 

  • Hernández, A., & Marcos, R. (2008). Genetic variations associated with interindividual sensitivity in the response to arsenic exposure. Pharmacogenomics, 9(8), 1113–1132.

    Article  Google Scholar 

  • Huang, R. N., & Lee, T. C. (1996). Cellular uptake of trivalent arsenite and pentavalent arsenate in KB cells cultured in phosphate-free medium. Toxicology and Applied Pharmacology, 136(2), 243–249.

    Article  Google Scholar 

  • Huang, Y., Zhang, J., McHenry, K. T., Kim, M. M., Zeng, W., Lopez-Pajares, V., et al. (2008). Induction of cytoplasmic accumulation of p53: A mechanism for low levels of arsenic exposure to predispose cells for malignant transformation. Cancer Research, 68(22), 9131–9136.

    Article  Google Scholar 

  • Hughes, M. F., Devesa, V., Adair, B. M., Conklin, S. D., Creed, J. T., Styblo, M., et al. (2008). Tissue dosimetry, metabolism and excretion of pentavalent and trivalent dimethylated arsenic in mice after oral administration. Toxicology and Applied Pharmacology, 227(1), 26–35.

    Article  Google Scholar 

  • IARC. (2012). Monographs on the Evaluation of Carcinogenic Risks to Humans, No. 100C. IARC Working Group on the Evaluation of Carcinogenic Risk to Humans. Lyon: International Agency for Research on Cancer.

    Google Scholar 

  • IARC. (2004). Monographs on the evaluation of carcinogenic risks to humans. Some Drinking-water Disinfectants and Contaminants, including Arsenic, 84. Lyon: IARC Scientific Publications 1-229.

    Google Scholar 

  • Islam, M. A., Sakakibara, H., Karim, M. R., Sekine, M., & Mahmud, Z. H. (2011). Bacteriological assessment of drinking water supply options in coastal areas of Bangladesh. Journal of Water and Health, 9(2), 415–428.

    Article  Google Scholar 

  • James, K. A., Byers, T., Hokanson, J. E., Meliker, J. R., Zerbe, G. O., & Marshall, J. A. (2015). Association between lifetime exposure to inorganic arsenic in drinking water and coronary heart disease in Colorado residents. Environmental Health Perspectives, 123(2), 128–134.

    Article  Google Scholar 

  • Johnston, R., Hug, S. J., Inauen, J., Khan, N. I., Mosler, H. J., & Yang, H. (2014). Enhancing arsenic mitigation in Bangladesh: Findings from institutional, psychological, and technical investigations. Science of Total Environment, 488–489, 477–483.

    Article  Google Scholar 

  • Khanjani, N., Jafarnejad, A. B., & Tavakkoli, L. (2017). Arsenic and breast cancer: A systematic review of epidemiologic studies. Reviews on Environmental Health, 32(3), 267–277.

    Article  Google Scholar 

  • Khuda-Bukhsh, A. R., Roy-Karmakar, S., Banerjee, A., Banerjee, P., Pathak, S., Biswas, S. J., et al. (2011). A follow-up study on the efficacy of the homeopathic remedy arsenicum album in volunteers living in high risk arsenic contaminated areas. Evidence-Based Complementary and Alternative Medicine, 2011, 129214.

    Article  Google Scholar 

  • Kim, Y. J., & Kim, J. M. (2015). Arsenic toxicity in male reproduction and development. Development and Reproduction, 19(4), 167–180.

    Article  Google Scholar 

  • Kyle, R. A., & Pease, G. L. (1965). Hematologic aspects of arsenic intoxication. New England Journal of Medicine, 273, 18–23.

    Article  Google Scholar 

  • Lam, S. H., Sin, Y. M., Gong, Z., & Lam, T. J. (2005). Effects of thyroid hormone on the developmentof immune system in zebrafish. General and Comparative Endocrinology, 142(3), 325–335.

    Article  Google Scholar 

  • Lee, R. C., & Kissel, J. C. (1995). Probabilistic prediction of exposures to arsenic contaminated residential soil. Environmental Geochemistry and Health, 17(4), 159–168.

    Article  Google Scholar 

  • Lee-Chen, S. F., Yu, C. T., & Jan, K. Y. (1992). Effect of arsenite on the DNA repair ofUV-irradiated Chinese hamster ovary cells. Mutagenesis, 7(1), 51–55.

    Article  Google Scholar 

  • Lemarie, A., Bourdonnay, E., Morzadec, C., Fardel, O., & Vernhet, L. (2008). Inorganic arsenicactivates reduced NADPH oxidase in human primary macrophages through a Rhokinase/p38 kinase pathway. Journal of Immunology, 180(9), 6010–6017.

    Article  Google Scholar 

  • Lemarie, A., Morzadec, C., Bourdonnay, E., Fardel, O., & Vernhet, L. (2006). Human macrophagesconstitute targets for immunotoxic inorganic arsenic. Journal of Immunology, 177(5), 3019–3027.

    Article  Google Scholar 

  • Lin, H. J., Sung, T. I., Chen, C. Y., & Guo, H. R. (2013). Arsenic levels in drinking water and mortality of liver cancer in Taiwan. Journal of Hazardous Materials, 262, 1132–1138.

    Article  Google Scholar 

  • Liu, F. P., Chen, X. H., Fu, M., & Chen, Y. (2002). Determination of arsenic in animal liver by atomic fluorescence spectrometry. Guang Pu Xue Yu Guang Pu Fen Xi, 22(3), 491–492.

    Google Scholar 

  • Lu, M., Wang, H., Li, X. F., Arnold, L. L., Cohen, S. M., & Le, X. C. (2007). Binding of dimethylarsinousacid to cys-13 alpha of rat hemoglobin is responsible for the retention of arsenic in rat blood. Chemical Research in Toxicology, 20(1), 27–37.

    Article  Google Scholar 

  • Maher, W. A. (1985). The presence of arsenobetaine in marine animals. Comparative Biochemistry Physiology C, 80(1), 199–201.

    Article  Google Scholar 

  • Majumder, B., Das, S., Mukhopadhyay, S., & Biswas, A. K. (2019). Identification ofarsenic-tolerant and arsenic-sensitive rice (Oryza sativa L.) cultivars on thebasis of arsenic accumulation assisted stress perception, morpho-biochemicalresponses, and alteration in genomic template stability. Protoplasma, 256(1), 193–211.

    Google Scholar 

  • Malik, J. A., Goel, S., Sandhir, R., & Nayyar, H. (2011). Uptake and distribution of arsenic in chickpea: Effects on seed yield and seed composition. Communication in Soil Science and Plant Analysis, 42, 1728–1738.

    Article  Google Scholar 

  • Mazumder, D. N. (2005). Effect of chronic intake of arsenic-contaminated water on liver. Toxicology and Applied Pharmacology, 206(2), 169–175.

    Article  Google Scholar 

  • Meliker, J. R., Slotnick, M. J., AvRuskin, G. A., Schottenfeld, D., Jacquez, G. M., Wilson, M. L., et al. (2010). Lifetime exposure to arsenic in drinkingwater and bladder cancer: a population-based case-control study in Michigan, USA.Cancer Causes and Control, 21(5), 745–757.

    Google Scholar 

  • Milton, A. H., Smith, W., Rahman, B., Hasan, Z., Kulsum, U., Dear, K., et al. (2005). Chronic arsenic exposure and adverse pregnancy outcomes in Bangladesh. Epidemiology, 16(1), 82–86.

    Google Scholar 

  • Milton, A. H., Smith, W., Rahman, B., Hasan, Z., Kulsum, U., Dear, K., et al. (2017). Low-level arsenic in drinking water and risk of incident myocardial infarction: A cohort study. Environmental Research, 154, 318–324.

    Article  Google Scholar 

  • Monrad, M., Ersbøll, A. K., Sørensen, M., Baastrup, R., Hansen, B., Gammelmark, A., et al. (2017). Low-level arsenic in drinking water and risk of incident myocardial infarction: A cohort study. Environmental Research, 154, 318–324.

    Article  Google Scholar 

  • Moon, K. A., Oberoi, S., Barchowsky, A., Chen, Y., Guallar, E., Nachman, K. E., et al. (2017). A dose-response meta-analysis of chronic arsenic exposure and incident cardiovascular disease. International Journal of Epidemiology, 46(6), 1924–1939.

    Google Scholar 

  • Moore, L. E., Smith, A. H., Hopenhayn-Rich, C., Biggs, M. L., Kalman, D. A., & Smith, M. T. (1997). Decrease in bladder cell micronucleus prevalence after intervention to lower the concentration of arsenic in drinking water. Cancer Epidemiology and Biomarker Prevention, 6(12), 1051–1056.

    Google Scholar 

  • Naujokas, M. F., Anderson, B., Ahsan, H., Aposhian, H. V., Graziano, J. H., Thompson, C., et al. (2013). The broad scope of health effects from chronic arsenic exposure: Update on a worldwide public health problem. Environmental Health Perspectives, 121(3), 295–302. https://doi.org/10.1289/ehp.1205875.

  • Nohara, K., Ao, K., Miyamoto, Y., Suzuki, T., Imaizumi, S., Tateishi, Y., et al. (2008). Arsenite-induced thymus atrophy is mediated by cell cycle arrest: A characteristic downregulation of E2F-related genes revealed by a microarray approach. Toxicological Sciences, 101(2), 226–238.

    Article  Google Scholar 

  • NRC (National Research Council). (2000). Arsenic in drinking water. Washington, DC: National Academy Press.

    Google Scholar 

  • NRC (National Research Council). (2001). Arsenic in drinking water. Washington, DC: National Academy Press.

    Google Scholar 

  • Patterson, R., Vega, L., Trouba, K., Bortner, C., & Germolec, D. (2004). Arsenic-induced alterations in the contact hypersensitivity response in Balb/c mice. Toxicology and Applied Pharmacology, 198(3), 434–443.

    Article  Google Scholar 

  • Rahman, A., Vahter, M., Smith, A. H., Nermell, B., Yunus, M., El Arifeen, S., et al. (2009). Arsenic exposure during pregnancy and size at birth: A prospective cohort study in Bangladesh. American Journal of Epidemiology, 169(3), 304–312.

    Article  Google Scholar 

  • Rana, S. V., & Allen, T. (2006). Influence of thyroxine and n-propylthiouracil on nephro-toxicity of inorganic arsenic in rat. Toxicology and Industrial Health, 22(3), 137–145.

    Article  Google Scholar 

  • Rose, M., Lewis, J., Langford, N., Baxter, M., Origgi, S., Barber, M., et al. (2007). Arsenic in seaweed–forms, concentration and dietary exposure. Food Chemical Toxicology, 45(7), 1263–1267.

    Article  Google Scholar 

  • Rossman, T. G., Meyn, M. S., & Troll, W. (1977). Effects of arsenite on DNA repair in Escherichia coli. Environmental Health Perspectives, 19, 229–233.

    Article  Google Scholar 

  • Samavarchi Tehrani, S., Mahmoodzadeh Hosseini, H., Yousefi, T., Abolghasemi, M., Qujeq, D., Maniati, M., et al. (2018). The crosstalk between trace elements with DNA damage response, repair, and oxidative stress in cancer. Journal of Cellular Biochemistry, 1–26. https://doi.org/10.1002/jcb.27617.

  • Sattar, A., Xie, S., Hafeez, M. A., Wang, X., Hussain, H. I., Iqbal, Z., et al. (2016). Metabolism and toxicity of arsenicals in mammals. Environmental Toxicology and Pharmacology, 48, 214–224.

    Article  Google Scholar 

  • Savabieasfahani, M., Lochmiller, R. L., Rafferty, D. P., & Sinclair, J. A. (1998). Sensitivity of wild cotton rats (Sigmodon hispidus) to the immunotoxic effects of low-level arsenic exposure. Archives of Environmental Contamination and Toxicology, 34(3), 289–296.

    Article  Google Scholar 

  • Schaumlöffel, N., & Gebel, T. (1998). Heterogeneity of the DNA damage provoked by antimony and arsenic. Mutagenesis, 13(3), 281–286.

    Article  Google Scholar 

  • Selzer, P. M., & Ancel, M. A. (1983). Chronic arsenic poisoning masquerading as pernicious anemia. The Western Journal of Medicine, 139(2), 219–220.

    Google Scholar 

  • Sen, J., & Chaudhuri, A. (2008). Arsenic exposure through drinking water and its effect on pregnancy outcome in Bengali women. Archives of Industrial Hygiene and Toxicology, 59(4), 271–275.

    Article  Google Scholar 

  • Sengupta, M., & Bishayi, B. (2002). Effect of lead and arsenic on murine macrophage response. Drug Chemical Toxicology, 25(4), 459–472.

    Article  Google Scholar 

  • Sharma, S., Gupta, A., Deshmukh, A., & Puri, V. (2016). Arsenic poisoning and Mees’ lines. QJM an International Journal of Medicine, 109(8), 565–566.

    Article  Google Scholar 

  • Shukla, N. P., & Pandey, G. N. (1985). Effect of heavy metals on fish–a review. Reviews on Environmental Health, 5(1), 87–99.

    Google Scholar 

  • Skröder, H., Engström, K., Kuehnelt, D., Kippler, M., Francesconi, K., Nermell, B., et al. (2018). Associations between methylated metabolites of arsenic and selenium in urine of pregnant Bangladeshi women and interactions between the main genes involved. Environmental Health Perspectives, 126(2), 027001.

    Google Scholar 

  • Soto-Peña, G. A., Luna, A. L., Acosta-Saavedra, L., Conde, P., López-Carrillo, L., Cebrián, M. E., et al. (2006). Assessment of lymphocyte subpopulations and cytokine secretion in children exposed to arsenic. Federation of American Societies for Experimental BiologyJournal, 20(6), 779–781.

    Article  Google Scholar 

  • Soto-Peña, G. A., & Vega, L. (2008). Arsenic interferes with the signalling transduction pathway of T cell receptor activation by increasing basal and induced phosphorylation of Lck and Fyn in spleen cells. Toxicology and Applied Pharmacology, 230(2), 216-226.

    Google Scholar 

  • Sun, H. J., Li, S. W., Li, C., Wang, W. Q., Li, H. B., & Ma, L. Q. (2017). Thyrotoxicity of arsenate and arsenite on juvenile mice at organism, sub-cellular, and gene levels under low exposure. Chemosphere, 186, 580–587.

    Article  Google Scholar 

  • Tolins, M., Ruchirawat, M., & Landrigan, P. (2014). The developmental neurotoxicity of arsenic: Cognitive and behavioural consequences of early life exposure. Annals of Global Health, 80(4), 303–314.

    Article  Google Scholar 

  • Vahidnia, A., van der Voet, G. B., & de Wolff, F. A. (2007). Arsenic neurotoxicity–a review. Human and Experimental Toxicology, 26(10), 823–832.

    Article  Google Scholar 

  • Vahter, M. (2002). Mechanisms of arsenic biotransformation. Toxicology, 181–182, 211–217.

    Article  Google Scholar 

  • Vahter, M. E. (2007). Interactions between arsenic-induced toxicity and nutrition in early life. Journal of Nutrition, 137(12), 2798–2804.

    Article  Google Scholar 

  • Vantroyen, B., Heilier, J. F., Meulemans, A., Michels, A., Buchet, J. P., Vanderschueren, S., et al. (2004). Survival after a lethal dose of arsenic trioxide. Journal of Toxicology: Clinical Toxicology, 42(6), 889–895.

    Google Scholar 

  • Vineetha, V. P., & Raghu, K. G. (2019). An overview on arsenic trioxide induced cardiotoxicity. Cardiovascular Toxicology, 19(2), 105–119.

    Google Scholar 

  • Vromman, D., Lutts, S., Lefèvre, I., Somer, L., De Vreese, O., Šlejkovec, Z., & Quinet, M. (2013). Effects of simultaneous arsenic and iron toxicities on rice (Oryza sativa L.) development, yield-related parameters and As and Fe accumulation in relation to As speciation in the grains. Plant and Soil, 371, 199–217.

    Article  Google Scholar 

  • Vu, V., Navalkar, N., & Wei, Y. (2019). Endocrine disrupting metals in ambient air and female breast cancer incidence in US. Gynecological Endocrinology, 35(12), 1099–1102.

    Article  Google Scholar 

  • Wade, T. J., Xia, Y., Mumford, J., Wu, K., Le, X. C., Sams, E., et al. (2015). Cardiovascular disease and arsenic exposure in Inner Mongolia, China: A case control study. Environmental Health, 14, 35.

    Google Scholar 

  • Wang, T. S., Shu, Y. F., Liu, Y. C., Jan, K. Y., & Huang, H. (1997). Glutathione peroxidase and catalase modulate the genotoxicity of arsenite. Toxicology, 121(3), 229–237.

    Article  Google Scholar 

  • Warner, M. L., Moore, L. E., Smith, M. T., Kalman, D. A., Fanning, E., & Smith, A. H. (1994). Increased micronuclei in exfoliated bladder cells of individuals who chronically ingest arsenic-contaminated water in Nevada. Cancer Epidemiology Biomarkers Prevention, 3(7), 583–590.

    Google Scholar 

  • Watson, W. H., & Yager, J. D. (2007). Arsenic: Extension of its endocrine disruption potential to interference with estrogen receptor-mediated signalling. Toxicological Sciences, 98(1), 1–4.

    Article  Google Scholar 

  • World Health Organization (WHO). (2001) Arsenic and arsenic compounds, 2nd Edn. Environmental Health Criteria 224. Geneva CH [updated 2001; accessed August 25, 2019]. Available from: https://www.inchem.org/documents/ehc/ehc/ehc224.htm.

  • Wu, L., Yi, H., & Yi, M. (2010). Assessment of arsenic toxicity using Allium/Vicia root tip micro nucleus assays. Journal of Hazardous Materials, 176(1–3), 952–956.

    Article  Google Scholar 

  • Yamamoto, S., Konishi, Y., Matsuda, T., Murai, T., Shibata, M. A., Matsui-Yuasa, I., et al. (1995). Cancer induction by an organic arsenic compound, dimethylarsinic acid (cacodylic acid), in F344/DuCrj rats afterpre-treatment with five carcinogens. Cancer Research, 55(6), 1271–1276.

    Google Scholar 

  • Yen, Y. P., Tsai, K. S., Chen, Y. W., Huang, C. F., Yang, R. S., & Liu, S. H. (2010). Arsenic inhibits myogenic differentiation and muscle regeneration. Environmental Health Perspectives, 118(7), 949–956.

    Article  Google Scholar 

  • Zadorozhnaja, T. D., Little, R. E., Miller, R. K., Mendel, N. A., Taylor, R. J., Presley, B. J., et al. (2000). Concentrations of arsenic, cadmium, copper, lead, mercury, and zinc in human placentas from two cities in Ukraine. Journal of Toxicology and Environmental Health A, 61(4), 255–263.

    Google Scholar 

  • Zakharyan, R. A., Wildfang, E., & Aposhian, H. V. (1996). Enzymatic methylation of arseniccompounds. III. The marmoset and tamarin, but not the rhesus, monkeys are deficient in methyl transferases that methylate inorganic arsenic. Toxicology and Applied Pharmacology, 140(1), 77–84.

    Google Scholar 

  • Zaroogian, G. E., & Hoffman, G. L. (1982). Arsenic uptake and loss in the American oyster, Crassostrea virginica. Environmental Monitoring and Assessment, 1(4), 345–358.

    Article  Google Scholar 

  • Zolot, J. (2016). Arsenic levels in drinking water linked to bladder cancer in News England. American Journal of Nursing, 116(8), 16.

    Article  Google Scholar 

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Acknowledgements

The authors sincerely acknowledge Department of Science and Technology, Govt. of India, DST-FIST (SR/FST/LS-I/2018/173) and DBT-BOOST No.118/14/BT(Estt)/1P-4/2013 for providing infrastructural support.

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Biswas, S.J. et al. (2021). Primary Concept of Arsenic Toxicity: An Overview. In: Adhikary, P.P., Shit, P.K., Santra, P., Bhunia, G.S., Tiwari, A.K., Chaudhary, B.S. (eds) Geostatistics and Geospatial Technologies for Groundwater Resources in India. Springer Hydrogeology. Springer, Cham. https://doi.org/10.1007/978-3-030-62397-5_16

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